Canonical Allele Identifier: CA353801095

Gene: BTLA

Linked Data

• MyVariant Identifiers: chr3:g.112185004T>C (hg19) ; chr3:g.112466157T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112466157T>C , CM000665.2:g.112466157T>C	GRCh38
NC_000003.11:g.112185004T>C , CM000665.1:g.112185004T>C	GRCh37
NC_000003.10:g.113667694T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334529.10:c.821A>G MANE Select	ENSP00000333919.5:p.Asn274Ser
ENST00000334529.9:c.821A>G	ENSP00000333919.5:p.Asn274Ser
ENST00000383680.4:c.677A>G	ENSP00000373178.4:p.Asn226Ser
ENST00000474965.1:n.325A>G
NM_001085357.1:c.677A>G	NP_001078826.1:p.Asn226Ser
NM_181780.3:c.821A>G	NP_861445.3:p.Asn274Ser
XM_011512446.1:c.839A>G	XP_011510748.1:p.Asn280Ser
XM_011512447.1:c.839A>G	XP_011510749.1:p.Asn280Ser
XM_011512447.3:c.839A>G	XP_011510749.1:p.Asn280Ser
XM_017005748.2:c.821A>G	XP_016861237.1:p.Asn274Ser
NM_181780.4:c.821A>G MANE Select	NP_861445.4:p.Asn274Ser
NM_001085357.2:c.677A>G	NP_001078826.1:p.Asn226Ser